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Antifungal susceptibility testing of yeasts: evaluation of technical variables for test automation.

机译:酵母菌的抗真菌药敏试验:评估自动化试验的技术变量。

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摘要

The technical parameters for antifungal susceptibility testing with Candida species were reexamined to determine the optimal conditions for testing with semiautomated preparations of broth microdilution cultures, automated spectrophotometric readings of the cultures, and dose-response and endpoint determinations by means of a computer spreadsheet. Tests were based on proposed standard method M27P of the National Committee for Clinical Laboratory Standards for antifungal agents. RPMI 1640 broth with extra glucose to a final concentration of 2% gave higher and more reproducible drug-free control readings without affecting susceptibility endpoint readings. An inoculum of 8 x 10(4) yeasts per ml prepared from a carbon-limiting broth culture without further standardization was found to give optimal control readings after 48 h of incubation at 37 degrees C. For flucytosine, fluconazole, itraconazole, and ketoconazole, endpoints based on 50% growth inhibition (50% inhibitory concentration) gave the minimum variation with inoculum size and the fewest endpoint differences with RPMI 1640 medium obtained from two different suppliers. The 50% inhibitory concentration was also the optimal endpoint for fluconazole and ketoconazole susceptibilities in comparison with broth macrodilution MICs determined by the method of the National Committee for Clinical Laboratory Standards. Intralaboratory reproducibility was determined by retrospective analysis of replicate results for isolates retested at random over a 2-year period. This approach showed less favorable reproducibility than has been reported from purpose-designed, prospective antifungal susceptibility studies, but it may better reflect real-life test reproducibility. Susceptibility data for 616 clinical isolates of yeasts, representing 16 Candida and Saccharomyces spp., confirmed the tendency of Candida lusitaniae isolates to show relatively low susceptibilities to amphotericin B, the tendency of Candida krusei isolates to show low flucytosine and fluconazole susceptibilities, and the presence of some isolates in the species Candida albicans, Candida glabrata, and Candida tropicalis with low susceptibilities to azole derivative antifungal agents. The study demonstrates the value of automation and standardization in all stages of yeast susceptibility testing, from plate preparation to data analysis.
机译:重新检查了念珠菌种类的抗真菌药敏试验的技术参数,以确定用肉汤微稀释培养物的半自动化制剂,培养物的自动分光光度读数以及通过计算机电子表格进行剂量反应和终点测定的最佳试验条件。测试基于抗真菌药物国家临床实验室标准委员会建议的标准方法M27P。最终葡萄糖浓度为2%的RPMI 1640肉汤含更高的葡萄糖,可以得到更高且可重复的无药物对照读数,而不会影响药敏终点读数。发现在无进一步标准化的情况下,由无碳限制的肉汤培养液制备的每毫升8 x 10(4)酵母菌接种物在37摄氏度下孵育48小时后可提供最佳对照读数。对于氟胞嘧啶,氟康唑,伊曲康唑和酮康唑,基于50%生长抑制(50%抑制浓度)的最终终点,接种量的变化最小,而从两个不同供应商处获得的RPMI 1640培养基的最终终点差异最小。与通过国家临床实验室标准委员会的方法确定的肉汤大量稀释MIC相比,50%抑制浓度也是氟康唑和酮康唑敏感性的最佳终点。实验室内的可重复性是通过对2年内随机重新测试的分离株的复制结果进行回顾性分析来确定的。与专门设计的前瞻性抗真菌药敏性研究报告的方法相比,该方法显示出较差的良好重现性,但它可能更好地反映了实际测试的重现性。代表16个念珠菌和酿酒酵母的616株临床酵母菌的药敏性数据证实了卢氏念珠菌对两性霉素B的敏感性较低,库鲁氏念珠菌对氟胞嘧啶和氟康唑的敏感性较低,并且存在白念珠菌,光滑念珠菌和热带念珠菌中的一些分离株对唑衍生物抗真菌剂的敏感性低。这项研究证明了自动化和标准化在从酶标制备到数据分析的酵母敏感性测试的所有阶段的价值。

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